Minimally Invasive Esophagectomy Pain Control Trial

Status Recruiting

Clinical Trial Summary

A pilot randomized controlled trial comparing intercostal nerve blocks, cryo-ablation plus intercostal nerve blocks, and serratus plane catheter plus intercostal nerve blocks in patients undergoing esophagectomies with minimally invasive thoracic approaches.

Clinical Trial Description

Pilot study planned to consent 30 patients in total with a projected study timeline of 2-3 years for completion. Participants will be enrolled in the study and randomized in their preoperative clinic visit. On the day of surgery, they will receive the intervention they were randomized to. 10 patients will be randomized to the intercostal block group, 10 patients will be randomized to the cryo-ablation plus intercostal block group, and 10 patients will be randomized to the serratus plane catheter plus intercostal block group. They will be followed throughout their hospital stay until discharge for data collection purposes. Once the patient is discharged from the hospital, post-operative follow-up in the Swedish Thoracic Surgery Clinic will be collected up to 1 year post-operatively. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05906134
Study type	Interventional
Source	Swedish Medical Center
Contact	Brian Louie, M.D.
Phone	(206) 215-6800
Email	brian.louie@swedish.org
Status	Recruiting
Phase	Phase 1/Phase 2
Start date	April 26, 2022
Completion date	February 2026

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